| Primary Device ID | G5103140 |
| NIH Device Record Key | 00556c9c-4c5c-4961-b082-8d048ca7583c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SOLAR BRONZE |
| Version Model Number | 3140 |
| Company DUNS | 075058495 |
| Company Name | Light Sources, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | G5103140 [Primary] |
| LEJ | Booth, Sun Tan |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-08 |
| Device Publish Date | 2024-12-31 |
| G51031480 | 3148 |
| G51031460 | 3146 |
| G51031380 | 3138 |
| G51031360 | 3136 |
| G51031430 | 3143 |
| G51031350 | 3135 |
| G5103142 | 3142 |
| G5103140 | 3140 |
| G5103141 | 3141 |
| G5103147 | 3147 |
| G5103145 | 3145 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SOLAR BRONZE 87942949 not registered Live/Pending |
JLW-TW Corp 2018-05-31 |
![]() SOLAR BRONZE 75208191 2130259 Dead/Cancelled |
Vickmark Industries, L.L.C. 1996-11-20 |